All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00025 614053 Mitochondrial complex V (ATP synthase) deficiency, nuclear type 3, 614053 (3) 614053 0 0 ATP5E, ATP5F1E - -